Bulletin of the Korean Chemical Society

  • 제32권6호
  • /
  • Pages.2070-2072
  • /
  • 2011
  • /
  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

Catalytic Oxidative Conversion of Aldehydes to Carboxylic Esters and Acids Under Mild Conditions

  • 투고 : 2011.04.18
  • 심사 : 2011.05.03
  • 발행 : 2011.06.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  1. Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis; John Wiley & Sons: New York, 1991.
  2. Otera, J. Esterification: Methods, Reactions and Applications; Wiley: New York, 2003.
  3. Ekoue-Kovi, K.; Wolf, C. Chem. Eur. J. 2008, 6302.
  4. De Sarker, S.; Grimme, S.; Studer, A. J. Am. Chem. Soc. 2010, 132, 1190. https://doi.org/10.1021/ja910540j
  5. Mitsukura, K.; Sato, Y.; Yoshida, T.; Nagasawa, T. Biotechnol. Lett. 2004, 26, 1643. https://doi.org/10.1007/s10529-004-3513-4
  6. Larock, R. C. Comprehensive Organic Transformations: A Guide to Functional Group Preparation; VCH: New York, 1989, p. 840
  7. William, D. R.; Klingler, F. D.; Allen, E. E.; Lichtenthaler, F. W. Tetrahedron Lett. 1988, 29, 5087. https://doi.org/10.1016/S0040-4039(00)80686-3
  8. O'Connor, B.; Just, G. Tetrahedron Lett. 1987, 28, 3235. https://doi.org/10.1016/S0040-4039(00)95480-7
  9. Qian, G.; Zhao, R.; Ji, D.; Lu, G.; Qi, Y.; Suo, J. Chem. Lett. 2004, 33, 834. https://doi.org/10.1246/cl.2004.834
  10. Sundararaman, P.; Walker, E. C.; Djerassi, C. Tetrahedron Lett. 1978, 19, 1627. https://doi.org/10.1016/S0040-4039(01)94623-4
  11. Travis, B. R.; Sivakumar, M.; Hollist, G. O.; Borhan, B. Org. Lett. 2003, 5, 1031. https://doi.org/10.1021/ol0340078
  12. McDonald, C.; Holcomb, H.; Kennedy, K.; Kirkpatrick, E.; Leathers, T.; Vanemon, P. J. Org. Chem. 1989, 54, 1213. https://doi.org/10.1021/jo00266a046
  13. Gopinah, R.; Barkakaty, B.; Talukdar, B.; Patel, B. K. J. Org. Chem. 2003, 68, 2944. https://doi.org/10.1021/jo0266902
  14. Thomason, S. C.; Kubler, D. G. J. Chem. Educ. 1968, 45, 546. https://doi.org/10.1021/ed045p546
  15. Lerebours, R.; Wolf, C. J. Am. Chem. Soc. 2006, 128, 13052. https://doi.org/10.1021/ja063476c
  16. Wei, L.-L.; Wei, L.-M.; Pan, W.-B.; Wu, M.-J. Synlett 2004, 1497.
  17. Murahashi, S.-I.; Naota, T.; Ito, K.; Maeda, Y.; Taki, H. J. Org. Chem. 1987, 52, 4319. https://doi.org/10.1021/jo00228a032
  18. Rajendram, S.; Trivedi, D. C. Synthesis 1995, 153.
  19. Grigg, R.; Mitchell, T. R. B.; Sutthivaiyakit, S. Tetrahedron 1981, 37, 4313. https://doi.org/10.1016/0040-4020(81)85027-2
  20. Yoo, W.-J.; Li, C.-J. Tetrahedron Lett. 2007, 48, 1033. https://doi.org/10.1016/j.tetlet.2006.11.169
  21. Chavan, S. P.; Danatle, S. W.; Gavande, C. A.; Venkataraman, M. S.; Praveen, C. Synlett 2002, 267.
  22. Kiyooka, S.; Ueno, M.; Ishii, E. Tetrahedron Lett. 2005, 46, 4639. https://doi.org/10.1016/j.tetlet.2005.04.093
  23. Kiyooka, S.-I.; Wada, Y.; Ueno, M.; Yokoyama, T.; Yokoyama, R. Tetrahedron 2007, 63, 12695. https://doi.org/10.1016/j.tet.2007.10.003
  24. Wu, X.-F.; Darcel, C. Eur. J. Org. Chem. 2009, 1144.
  25. Schmidt, A.; Habeck, T; Snovydovych, B.; Eisfeld, W. Org. Lett. 2007, 9, 3515. https://doi.org/10.1021/ol0713739
  26. Sakar, S. D.; Grimme, S.; Studer, A. J. Am. Chem. Soc. 2010, 132, 1190. https://doi.org/10.1021/ja910540j
  27. Victor Paul Raj, I.; Sudalai, A. Tetrahedron Lett. 2005, 46, 8303. https://doi.org/10.1016/j.tetlet.2005.09.173
  28. Castells, J.; Pujol, P. Tetrahedron 1982, 38, 337. https://doi.org/10.1016/0040-4020(82)80170-1
  29. Sessler, J. L.; Cho, D.-G. Org. Lett. 2008, 10, 73. https://doi.org/10.1021/ol7027306
  30. Cho, D.-G.; Kim, J. H.; Sessler, J. L. J. Am. Chem. Soc. 2008, 130, 12163. https://doi.org/10.1021/ja8039025
  31. Fontaine, P.; Chiaroni, A.; Masson, G.; Zhu, J. Org. Lett. 2008, 10, 1509. https://doi.org/10.1021/ol800199b

피인용 문헌

  1. ChemInform Abstract: Catalytic Oxidative Conversion of Aldehydes to Carboxylic Esters and Acids under Mild Conditions. vol.42, pp.43, 2011, https://doi.org/10.1002/chin.201143034
  2. Beyond Benzoin Condensation: Trimerization of Aldehydes via Metal-Free Aerobic Oxidative Esterification of Aldehydes with Benzoin Products in the Presence of Cyanide vol.16, pp.9, 2014, https://doi.org/10.1021/ol5008845
  3. Metal-Free Aerobic Oxidative Esterification of Aldehydes in the Presence of Cyanide vol.36, pp.8, 2015, https://doi.org/10.1002/bkcs.10398
  4. Synthesis and biological evaluation of novel SIPI-7623 derivatives as farnesoid X receptor (FXR) antagonists pp.1573-501X, 2019, https://doi.org/10.1007/s11030-018-9843-2
  5. Exo ⇔ Endo Isomerism, MEP/DFT, XRD/HSA-Interactions of 2,5-Dimethoxybenzaldehyde: Thermal, 1BNA-Docking, Optical, and TD-DFT Studies vol.25, pp.24, 2011, https://doi.org/10.3390/molecules25245970
  6. Cyanide Anions as Nucleophilic Catalysts in Organic Synthesis vol.53, pp.19, 2011, https://doi.org/10.1055/a-1499-8943